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Results 41-50 of 72 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
1996Structure and sequence of the human sulphamidase geneKarageorgos, L.; Guo, X.H.; Blanch, L.; Weber, B.; Anson, D.; Scott, H.; Hopwood, J.
1995In vivo delivery of human α-L-iduronidase in mice implanted with neo-organsSalvetti, A.; Moullier, P.; Cornet, V.; Brooks, D.; Hopwood, J.; Danos, O.; Heard, J.M.
1996Correction of Sanfilippo a Skin Fibroblasts By Retroviral Vector-Mediated Gene TransferBielicki, J.; Hopwood, J.; Anson, D.
1997Molecular defects in Sanfilippo syndrome type ABlanch, L.; Weber, B.; Guo, X.H.; Scott, H.; Hopwood, J.
1997A membrane protein primarily associated with the lysosomal compartmentBrooks, D.; Bradford, T.; Carlsson, S.; Hopwood, J.
1995Cloning of the sulphamidase gene and identification of mutations in Sanfilippo A syndromeScott, H.; Blanch, L.; Guo, X.H.; Freeman, C.; Orsborn, A.; Baker, E.; Sutherland, G.; Morris, C.; Hopwood, J.
1997Canine fucosidosis: a model for retroviral gene transfer into haematopoietic stem cellsFerrara, M.; Occhiodoro, T.; Fuller, M.; Hawthorne, W.; Teutsch, S.; Tucker, V.; Hopwood, J.; Stewart, G.; Anson, D.
1997Effect of enzyme replacement therapy on bone formation in a feline model of mucopolysaccharidosis Type VIByers, S.; Nuttall, J.; Crawley, A.; Hopwood, J.; Smith, K.; Fazzalari, N.
1999Sanfilippo type B syndrome (mucopolysaccharidosis III B): allelic heterogeneity corresponds to the wide spectrum of clinical phenotypesWeber, B.; Guo, X.H.; Kleijer, W.; van de Kamp, J.; Poorthuis, B.; Hopwood, J.
1995Isolation and characterisation of a recombinant precursor form of lysosomal acid α-glucosidaseFuller, M.; Van der Ploeg, A.; Reuser, A.; Anson, D.; Hopwood, J.

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